Gene
|
Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
|
6689 |
Gene nameGene Name - the full gene name approved by the HGNC.
|
Spi-B transcription factor |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
|
SPIB |
SynonymsGene synonyms aliases
|
SPI-B |
ChromosomeChromosome number
|
19 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
|
19q13.33 |
SummarySummary of gene provided in NCBI Entrez Gene.
|
The protein encoded by this gene is a transcriptional activator that binds to the PU-box (5`-GAGGAA-3`) and acts as a lymphoid-specific enhancer. Four transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep |
miRNAmiRNA information provided by mirtarbase database.
|
|
Transcription factors
|
Transcription factor |
Regulation |
Reference |
POU2AF1 |
Unknown |
24801987 |
POU2F2 |
Unknown |
24801987 |
|
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
|
|
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
|
|
Protein
|
UniProt ID |
Q01892 |
Protein name |
Transcription factor Spi-B |
Protein function |
Sequence specific transcriptional activator which binds to the PU-box, a purine-rich DNA sequence (5'-GAGGAA-3') that can act as a lymphoid-specific enhancer. Promotes development of plasmacytoid dendritic cells (pDCs), also known as type 2 DC p |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00178 |
Ets |
170 → 252 |
Ets-domain |
Domain |
|
Sequence |
|
Sequence length |
262 |
Interactions |
View interactions |
Associated diseases
|
Causal |
Disease name |
Disease term |
dbSNP ID |
References |
Liver failure |
Liver Failure |
rs118203990, rs118203991, rs118203992, rs387907022, rs201861847, rs796065037, rs759315662, rs368196005, rs796052121, rs369437593, rs367683258, rs766314948, rs368085185, rs770446752, rs753039116, rs776797592, rs1490906786, rs1562849964, rs759960319, rs776597537, rs375350359, rs1573008071, rs1601977105, rs1174791046, rs1019313682 |
|
Osteoporosis |
Osteoporosis |
rs72658152, rs72667023, rs587776916, rs72656370, rs768615287 |
|
|
Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Biliary cholangitis |
Primary biliary cholangitis, Secondary Biliary Cholangitis |
|
20639880 |
Biliary cirrhosis |
Biliary cirrhosis, Biliary Cirrhosis, Primary, 1, Primary biliary cirrhosis |
|
20639880, 21399635, 20639880, 21399635, 20639880, 26394269 |
Celiac disease |
Celiac Disease |
rs2305764, rs35218876 |
|
Cirrhosis |
Cirrhosis |
rs119465999, rs144369314, rs8056684, rs112053857, rs75998507 |
|
Conjugated hyperbilirubinemia |
Conjugated hyperbilirubinemia |
|
|
Dermatographic urticaria |
Dermatographic urticaria |
|
|
Gastrointestinal inflammation |
Gastrointestinal inflammation |
|
|
Hypoalbuminemia |
Hypoalbuminemia |
|
|
Liver carcinoma |
Liver carcinoma |
|
|
Liver fibrosis |
Fibrosis, Liver |
|
|
Portal hypertension |
Portal Hypertension |
|
|
|